Bisacodyl

Product NDC
24689-129
11-digit product format
246890129
Labeler code
24689
Product ID
24689-129_ec9edf75-b9cd-0b99-e053-2995a90a391f
Type
HUMAN OTC DRUG
Nonproprietary name
Bisacodyl
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Apnar Pharma LP
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-11-21
Marketing end
0000-00-00
Substance
BISACODYL
Active strength
5 mg/1
Pharmacologic classes
Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24689-129-02EA - Each24689-129d24bdef5-ae1b-49be-88a6-edcc20744c5a12023-04-07
24689-129-03EA - Each24689-1294f164bea-54d0-462e-a404-856b61008cef12023-04-07
24689-129-05EA - Each24689-1290dd342b2-74b9-4cc2-a66e-c1523f4cce9812023-03-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
24689-129-022468901290220 TABLET, DELAYED RELEASE in 1 BOTTLE (24689-129-02) 2022-11-210000-00-00NoNoCurrent
24689-129-0324689012903100 TABLET, DELAYED RELEASE in 1 BOTTLE (24689-129-03) 2022-11-210000-00-00NoNoCurrent
24689-129-0424689012904250 TABLET, DELAYED RELEASE in 1 BOTTLE (24689-129-04) 2022-11-210000-00-00NoNoCurrent
24689-129-0524689012905500 TABLET, DELAYED RELEASE in 1 BOTTLE (24689-129-05) 2022-11-210000-00-00NoNoCurrent